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Delphine RAMOS

VAKENBURG

En résumé

Installée depuis presque 20 ans aux Pays Bas, c''est un stage, puis ma these qui m'y ont amenée et mon mari hollandais qui m'y a fait rester. Je parle couramment le Néerlandais et l'Anglais, le Français étant ma langue natale.
Après ma thèse en Chimie organique, j'ai découvert le monde du développement pharmaceutique et m'y suis spécialisée. J'ai 14 ans d'expérience en Project/Program Management et Product Development. J'ai géré de gros Projets/Programmes avec des équipes multi-disciplinaires, parfois internationales.
Je me suis mise à mon compte en début d'année et suis à la recherche de postes intérim dans le domaine de project management et développement de produits pharmaceutiques. Je peux aussi vous aider à améliorer la performance de vos équipes basé sur une analyse rapide de votre organisation. Vous pouvez me contacter à cette adresse: info@cominsens.nl

Mes compétences :
Conseil
Coaching d'équipe
Management
Développement produit
Stratégie
Planning stratégique
Gestion de projet

Entreprises

  • ComInSenS - Owner, Freelance Project Manager & Advisor

    2016 - maintenant Deliver Project-, Program- & Team Management services, as well as Product Development services to Life Sciences companies.
    Focus on organization and structure to generate dedicated and aligned teams in order to reach optimal and sustainable performance.

  • Sanquin - Program Manager CEP

    2014 - 2015 Lead the Compliance Enhancement Program (CEP) designed to lift the Compliance hold (US).
    • Lead a cross-functional team across two sites (NL&BE); Align projects & sites.
    • Execute a pre-defined plan. Evaluate and revise plan upon performance.
    • Build a structure and develop processes enabling the management of the program.
    • Build the planning and manage the recruitment of external resources. Responsible for the budget.
    • Report progress to the Sr Management and the FDA.

  • HAL Allergy - Program Manager

    2008 - 2013 Lead the development program for the registration of 4 commercially available products in the context of a newly regulated environment (Allergy, immunotherapy).
    • Establish the program strategy, schedule & budget.
    • Execute the program according to plan. 3 multi-country Phase II studies performed within 2 years.
    • Lead cross-functional teams and Project Managers.
    • Set-up of the Project Management Office and matrix structure to enable the execution of the strategic programs (registration, new products, site transfer).

  • OctoPlus - Program Manager

    2007 - 2008 Lead the development program of 2 pharmaceutical products based on proprietary drug delivery technologies. Early stage development.

  • OctoPlus - Team Leader

    2005 - 2007 Set-up and management of a pre-clinical R&D group (10 professionals) to perform feasibility studies and early development programs including pre-clinical safety

  • OctoPlus - Project Leader/Scientist

    2001 - 2005 Development & evaluation of novel drug delivery technologies for the delivery of proteins, peptides and small molecules for OctoPlus or third parties.

  • Unilever - Thesarde

    Rueil-Malmaison 1996 - 2000 Subject: “A Novel Convergent Approach towards the Chemo-Enzymatic Synthesis of Neoglycopeptides”
    Doctorate: 1st December 2000
    Promotors: Prof. Dr. W. Klaffke & Prof. Dr. P. Rollin

    During this period, extensive experience was gained in chemical and enzymatic synthesis, carbohydrate and peptide chemistry, kinetic studies (microbial transglutaminase), NMR and Mass spectrometry analysis, chromatography column purification. I also learned organising and planning a project, supervising students and technicians, writing reports and articles, presenting results.

Formations

Réseau

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